FDA News Releases

• Date Index

• Country Life Natural Foods Conducts Nationwide Recall Of Peanut-Containing Candies Because Of Possible Health Risk (February 4), U.S. Food & Drug Administration (FDA)
• Braum's Ice Cream and Dairy Stores Announces Voluntary Recall of its Premium Ice Cream Flavor "Peanut Butter Pretzel" Following Expanded FDA Investigation of Peanut Corporation of America (February 3), U.S. Food & Drug Administration (FDA)
• ETHEX Corporation Issues Voluntary Nationwide Recall (February 3), U.S. Food & Drug Administration (FDA)
• Marathon Ventures, Inc. announces recall of dry, roasted peanuts (foodservice pack) and Bridge Mix due to possible health risk (February 3), U.S. Food & Drug Administration (FDA)
• JL Manufacturing Announces Recall Of Candies Containing Peanuts Because Of Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• T F Processors Inc. Recalls Double Fudge Peanut Butter Brownies Because of Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Blue Ribbon Products Inc., Announces Voluntary Recall of Ultimate Gourmet Peanut Butter Cookie Dough Due to Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Dutch Valley Food Development, Inc. Announces a Voluntary Nationwide Recall of Peanut Products made with Recalled Peanuts (February 3), U.S. Food & Drug Administration (FDA)
• FDA Issues Early Communication about a Safety Review of Xigris, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Xigris (Drotrecogin alfa):Early Communication about an Ongoing Safety Review re: increased bleeding events/mortality, U.S. Food & Drug Administration (FDA)
• MedWatch - Ethex Corp. recalls prescription prenatal vitamin and iron supplement products, U.S. Food & Drug Administration (FDA)
• Aurora Products Inc. Announces Voluntary Recall of Products Containing Roasted Peanuts Produced Under Aurora Natural Brand Due to Possible Peanut Corporation of America (PCA) Contamination and Potential Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• GKI Foods Inc. Expands Nationwide Recall of Peanut-Containing Candies Because of Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Grand Rapids Popcorn Recalls PCA's 30# Cases of Medium Chop Granulated Peanuts Sold in Michigan and Florida Because of Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Hershey Import Company Announces Nationwide Voluntary Recall on Certain Snacks (February 2), U.S. Food & Drug Administration (FDA)
• Kerry Ingredients and Flavours Announces Voluntary Recall of Choco Fudge Peanut Ingredient Following Expanded FDA Investigation of Peanut Corporation of America (February 2), U.S. Food & Drug Administration (FDA)
• Palmer Candy Company Announces Voluntary Recall of Blanched Salted Products Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• CVS/pharmacy Announces Voluntary Recall of Gold Emblem Brand Candy Containing Peanuts (February 3), U.S. Food & Drug Administration (FDA)
• Palmer Candy Company Announces A Nationwide Voluntary Recall of French Burnt Peanut and Boston Baked Bean Products Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Allegro Fine Foods, Inc. Recalls Wow Thai Peanut Wing Sauce and Dressing Because of Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Bear Stewart Corporation Announces Recall of Bear's Peanut Butter and Vegan Peanut Butter Cookies in All Sizes (February 2), U.S. Food & Drug Administration (FDA)
• Georgia Peanut Commission Recalls 11 oz. and 4 lb. Cans of Skinless and Honey Roasted Peanut Product Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Nutrition Research Group/Advanced Nutrient Science Announces Nationwide Voluntary Recall of Triple Delicious, All Natural Mega Protein and Oh Soo Good Bars (January 31), U.S. Food & Drug Administration (FDA)
• Stewart's Shops Recalls Caramel Candy Bar Dip Ice Cream Because of Possible Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Nut Bar Company Recalls Candy Shoppe Double Dip Peanuts Sold At Meijer Stores In Illinois, Indiana, Kentucky, Michigan And Ohio Because of Possible Health Risk. (February 3), U.S. Food & Drug Administration (FDA)
• Pecan Deluxe Candy Company Announces Nationwide Voluntary Recall of Certain Peanut Containing Products (Updated Information) (February 2), U.S. Food & Drug Administration (FDA)
• Thrift Products Recalls Thrifty Nut Brand Honey Roasted and Dry Roasted Peanuts Sold in Michigan And Indiana Because of Possible Risk To Health (February 3), U.S. Food & Drug Administration (FDA)
• GloryBee Foods, Inc. announces nationwide recall of Honey Roasted Peanut Splits, Whole Raw Blanched Peanuts, Organic Dry Roasted (No Salt) Peanut Splits, Conventional Dry Roasted (No Salt) Peanut Splits, Dry Roasted Granulated Medium Peanuts, Whole Honey Peanuts, Aunt Patty's Cascade Trail Mix (bulk, U.S. Food & Drug Administration (FDA)
• Bindi North America Announces Nationwide Recalls of Peanut Butter Gelato, Dream Bomba, and Peanut Butter Cheesecakes Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Forward Foods LLC Announces Voluntary Nationwide Recall of DETOUR Branded Bars Containing Roasted Peanuts Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• ISS Research Announces Voluntary Recall of OhYeah! Bars Due To Potential Health Risk (February 3), U.S. Food & Drug Administration (FDA)
• Austinuts Wholesale, Inc. Announces Voluntary Recall Of Honey Roasted Peanuts And Sweet and Spicy Snack Mix (February 3), U.S. Food & Drug Administration (FDA)
• Cherrydale Manufacturing LLC Recalls Bartons, Cherrydale Farms And Haddington Farms Products That Contain Peanuts Because Of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Earth Island Announces Voluntary Recall on Select Follow Your Heart Deli Products That Contain Peanut Butter Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Walgreens Recalls Cafe W Brand Trail Mix Containing Peanuts (February 2), U.S. Food & Drug Administration (FDA)
• Hain Celestial Voluntarily Issues Nationwide Expanded Recall of Certain Ethnic Gourmet Chicken Pad Thai Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Umpqua Dairy issues Voluntary Recall on its Tin Roof Sundae Ice Cream products Due to Expanded Peanut Recall by Peanut Corporation of America (PCA) (February 2), U.S. Food & Drug Administration (FDA)
• Crown Pacific Fine Foods Recalls Roasted Honey Peanuts, Virginia Roasted/Salted Peanuts, Virginia Roasted No Salt Peanuts, Roasted/Salted Peanuts, Roasted/Unsalted Peanuts Because of Health Risk Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Hudsonville Ice Cream Announces a Recall of Candy Bar Whirl Ice Cream Distributed in Indiana, Michigan, and Ohio Because of Possible Risk to Health (February 2), U.S. Food & Drug Administration (FDA)
• Prairie Farms Dairy Announces Voluntary Nationwide Recall Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Landies Candies Co. Inc Expands Voluntary Recall to Include Select Organic Peanut Clusters Due to Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Ocean Spray Announces Nationwide Voluntary Recall of 1.75 oz and 48 oz Fruit and Nut Trail Mix Products (February 2), U.S. Food & Drug Administration (FDA)
• Kashi Initiates Nationwide Recall of Select Kashi TLC Chewy Granola Bar Flavors And Kashi TLC Chewy Cookie Flavors (February 2), U.S. Food & Drug Administration (FDA)
• Tropical Nut And Fruit Recalls Granulated Peanuts Because of Possible Health Risk(February 2), U.S. Food & Drug Administration (FDA)
• Kellogg Company Announces Voluntary Nationwide Recall of Select Keebler Soft Batch Cookies and Special K Protein Meal Bar Honey Almond Flavor and Expansion of the 01/16/09 Recall of Various Crackers and Cookies February 2), U.S. Food & Drug Administration (FDA)
• Generic Drug Roundup: February 2009, U.S. Food & Drug Administration (FDA)
• Caribou Coffee Participates in Voluntary Nationwide Peanut Product Recall (January 30), U.S. Food & Drug Administration (FDA)
• Multiple Brands of Tin Roof Sundae Ice Cream Recalled as Part of Nationwide Peanut Corporation of America Recall(January 31), U.S. Food & Drug Administration (FDA)
• Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
  • Recalls, Market Withdrawals and Safety Alerts Update, U.S. Food & Drug Administration (FDA)
• Eillien's Candies, Inc. Issues Voluntary Recall of Select Peanut Candy Products Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Werner Gourmet Meat Snacks Inc. Recalls Trail Mixes and Peanut Items Because of Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• GKI Foods Inc. Initiates Nationwide Recall of Peanut-Containing Candies Because of Possible Health Risk (February 2), U.S. Food & Drug Administration (FDA)
• Genisoy Food Company Announces Voluntary Recall of Genisoy Organic Apple Cinnamon Soy Protein Bars Due to Potential Health Risk (February 1), U.S. Food & Drug Administration (FDA)
• Walgreens Recalls Walgreens Brand Candy Containing Peanuts Sold From Jan. 1, 2007 To Jan. 29, 2009 (February 1), U.S. Food & Drug Administration (FDA)
• Rucker's Candy Announces Voluntary Recall for Customer Private Labeled Products Including The Family Choice Labeled Brand (January 31), U.S. Food & Drug Administration (FDA)
• Velvet Ice Cream Pulling Cone Products (January 30), U.S. Food & Drug Administration (FDA)
• Pecan Deluxe Candy Company Announces Nationwide Voluntary Recall of Certain Peanut Containing Products (February 2), U.S. Food & Drug Administration (FDA)
• Kroger Recalls Peanut Butter Bakery Cookies and Select Cakes Due to Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Hain Celestial Voluntarily Issues Nationwide Recall of Certain Ethnic Gourmet Pad Thai And Kung Pao Frozen Food Products, and Certain Gluten Free Cafe Asian Curry Products, Because of Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Bass Pro Shops Announces Voluntary Nationwide Recall of Uncle Bucks Burnt Peanut Candy, No Sugar Added Chocolate Peanuts and No Sugar Added Peanut Clusters Due to Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Round Top Sundae Cones (January 29), U.S. Food & Drug Administration (FDA)
• Schwan Voluntarily Recalls Ice Cream Citing Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Standard Candy announces Voluntary Recall of Goo Goo Cluster and Goo Goo Peanut Butter because of possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• East Side Entrees Voluntarily Recalls Peanut Butter and Jelly Meal Breaks Because of Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Zachary Confections, Inc. Announces a Nationwide Voluntary Recall of Market Pantry Chocolate Covered Peanuts (January 31), U.S. Food & Drug Administration (FDA)
• Zachary Confections, Inc. Announces Nationwide Recall of Double Dipped Peanuts, Chocolate Peanuts, Bridge Mix, Caramel Nut Clusters, and Peanut Clusters due to Possible Peanut Corporation of America (PCA) Contamination and Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Best Brands Corp. Expands Voluntary Recall of Peanut Butter Frozen Cookie Dough (January 30), U.S. Food & Drug Administration (FDA)
• Mountain Man Nut and Fruit Co. Announces Nationwide Voluntary Recall of Select Products Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Kemps LLC Recalls Ice Cream Products (January 30), U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Produce Snacks (January 30), U.S. Food & Drug Administration (FDA)
• Weis Markets Announces Voluntary Recall of Seven Ice Cream Products Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Nature's Path Announces an Expanded Recall of Peanut Butter Optimum Energy Bars Nationwide Due to Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Bear Naked Announces Recall of Appalachian Trail Mixes Due to Possible Peanut Corporation of America Contamination and Potential Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• Pierre's Ice Cream Company Issues Voluntary Recall on its Pierre's Brand Sundae-Cone Style Products Due to Expanded Peanut Recall by Peanut Corporation of America (PCA) (January 30), U.S. Food & Drug Administration (FDA)
• Salix, LLC Recalls 6" Peanut Butter Filled Shank Bone Because Of Possible Salmonella Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Ice Cream Specialties Announces Nationwide Recall of Ice Cream Novelties Because of Possible Health Risk (January 31), U.S. Food & Drug Administration (FDA)
• HP Hood LLC Recalls Ice Cream Products (January 30), U.S. Food & Drug Administration (FDA)
• Harry and David Recalls Olympia Delight Trail Mix Because of Possible Health Risk (January 29), U.S. Food & Drug Administration (FDA)
• Clif Bar and Company Expands Its Voluntary Nationwide Recall Of CLIF and LUNA Branded Bars Containing Peanut Butter (January 30), U.S. Food & Drug Administration (FDA)
• Kroger Recalls Nut Topping Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Perry's Ice Cream Company Adds Products to Voluntary Recall of Select Peanut Butter Ice Cream Products as a result of PCA Expanded Recall (January 30), U.S. Food & Drug Administration (FDA)
• Wells' Dairy Expands Voluntary Recall of Select Blue Bunny Products (January 30), U.S. Food & Drug Administration (FDA)
• Lesserevil Brand Snack Co. Issues a Nationwide Voluntary Recall of Lesserevil Brand Peanut Butter and Choco Kettle Corn (January 30), U.S. Food & Drug Administration (FDA)
• House of Flavors Issues Voluntary Recall in Eastern United States Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Turkey Hill Dairy Announces Voluntary Recall of Select Ice Cream Flavors Following Expanded FDA Investigation of Peanut Corporation of America (January 30), U.S. Food & Drug Administration (FDA)
• NutriSystem Expands Voluntary United States Recall of Peanut Butter Granola Breakfast Bar to Include Canada Due to Possible Peanut Corporation Of America (PCA) Contamination and Potential Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Arico Natural Foods Company Announces US and Canadian Recall of Arico Peanut Butter Cookies and Cookie Bars Because of Possible Health Risk (January 29), U.S. Food & Drug Administration (FDA)
• Voluntary Recall Alert: Chef Pierre Chocolate Peanut Butter Silk Pie (January 30), U.S. Food & Drug Administration (FDA)
• Orchard Valley Harvest Announces Urgent Nationwide Voluntary Recall for Peanuts Because of Possible Health Risk (January 29), U.S. Food & Drug Administration (FDA)
• Rain Creek Baking Corporation Announces An Expanded Voluntary Withdrawal of Peanut Butter Turtles, Peanut Butter Baskets and Peanut Butter Princesses Due to Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Select Simbree Energy Foods Products Recalled Because of Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Galliker Dairy Announces Voluntary Recall of Rocky Road Ice Cream and Sundae Nut Cones Because of Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Country Maid Expands Upon Previous Voluntary Nationwide Recall of Classic Breaks Peanut Butter Cookie Dough Due to Possible Health Risk (January 29), U.S. Food & Drug Administration (FDA)
• Hy-Vee Inc. recalls two bakery products with peanuts distributed in seven states due to possible health risk (January 29), U.S. Food & Drug Administration (FDA)
• Meijer Announces Voluntary Recall for Some Meijer Brand Peanuts and Ice Cream Novelties Citing Possible Health Risk (January 30), U.S. Food & Drug Administration (FDA)
• Cropwell Bishop Creamery Limited Recalls Cheese Products Because of Possible Health Risk (January 26), U.S. Food & Drug Administration (FDA)
• Fieldbrook Foods Corp. Announces Nationwide Voluntary Recall of Select Ice Cream Novelty Products Due to Possible Health Risk (January 29), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - November 2008 Drug Safety Labeling Changes for 29 Drugs Now Available on Web, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets, Inc. Recalls Three Bakery Products with Peanuts (January 29), U.S. Food & Drug Administration (FDA)
• Wells' Dairy Announces Voluntary Recall of Select Blue Bunny Products Because of Possible Health Risk (January 29), U.S. Food & Drug Administration (FDA)
• Uncle Eddies Vegan Cookies Announces Recall of Uncle Eddies Vegan Peanut Butter Chocolate-Chip Cookies Because of Possible Health Risk (January 28), U.S. Food & Drug Administration (FDA)
• Peanut Corporation of America Expands Nationwide Recall of Peanut Products (January 28), U.S. Food & Drug Administration (FDA)
• House of Flavors Issues Allergy Alert for Undeclared Walnuts in Hanniford Chocolate Chip Ice Cream Sold at Sweetbay Supermarkets in Florida (January 28), U.S. Food & Drug Administration (FDA)
• MedWatch - Nationwide recall of multiple ETHEX generic drug products due to manufacturing deficiencies, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 28, 2009, U.S. Food & Drug Administration (FDA)
• ETHEX Corporation Issues Nationwide Voluntary Recall of Products (January 28), U.S. Food & Drug Administration (FDA)
• Ther-Rx Corporation Issues Nationwide Voluntary Recall of Products (January 28), U.S. Food & Drug Administration (FDA)
• Isagenix Announces Voluntary Recall of Chocolate Dipped Honey Peanut IsaLean Bar Due to Possible Peanut Corporation of America (PCA) Contamination and Potential Health Risk (January 27), U.S. Food & Drug Administration (FDA)
• Jenny Craig Announces Nationwide Voluntary Recall of Jenny's Cuisine Anytime Peanut Butter Flavor Nutritional Bars Due to Possible Peanut Corporation of America (PCA) Contamination and Potential Health Risk (January 27), U.S. Food & Drug Administration (FDA)
• Salix Voluntarily Recalls Dog Treat Due to Possible Health Risk (January 23), U.S. Food & Drug Administration (FDA)
• Carolina Prime Pet Announces Nationwide Recall of Dog Treats (January 27), U.S. Food & Drug Administration (FDA)
• ALDI Statement Regarding Peanut Butter Products Recall (January 23), U.S. Food & Drug Administration (FDA)
• Creative Energy Foods, Inc. Recalls Nutrition Bars Due To Possible Health Risk (January 21), U.S. Food & Drug Administration (FDA)
• MedWatch - Venom HYPERDRIVE 3.0 contains undeclared sibutramine, poses risks for abuse, addiction, and increased blood pressure and heart rate, U.S. Food & Drug Administration (FDA)
• SOPAKCO, Inc. Announces a Nationwide Recall of Certain SURE-PAK 12 Meals Containing Peanut Butter Products (January 27), U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers Against Dietary Supplement Containing Undeclared Drug, U.S. Food & Drug Administration (FDA)
• Falcon Trading Company/SunRidge Farms Withdraws Naturally Preferred Honey Nut Nuggets (January 23), U.S. Food & Drug Administration (FDA)
• Falcon Trading Company/SunRidge Farms Withdraws Certain Lots of SunRidge Tropical Golden Nuggets, SunRidge Chocolate Energy Bars and SunRidge Energy Nuggets (January 23), U.S. Food & Drug Administration (FDA)
• MedWatch - Plavix [Clopidogrel bisulfate] FDA safety review to evaluate differences in efffectiveness, genetic factors, potential drug interactions, U.S. Food & Drug Administration (FDA)
• Trader Joe's Expands Its Voluntary Recall To Include Trader Joe's Sliced Green Apples With All Natural Peanut Butter (January 23), U.S. Food & Drug Administration (FDA)
• Supreme Protein Voluntarily Recalls Supreme Protein brand Peanut Butter Crunch Bars and Caramel Nut Bars (January 23), U.S. Food & Drug Administration (FDA)
• Voluntary Recall Issued for ShopRite Peanut Butter on Toasty Crackers and ShopRite Peanut Butter and Cheese Cracker Snacks Because of Possible Health Risk (January 24), U.S. Food & Drug Administration (FDA)
• Stonewall Kitchen Voluntarily Recalls Seven Dessert Sauces (January 23), U.S. Food & Drug Administration (FDA)
• General Mills Issues Voluntary Recall of LARABAR and JamFrakas Peanut Butter Snack Bars (January 19), U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Whole Foods Carob Energee Nuggets (January 23), U.S. Food & Drug Administration (FDA)
• Brent and Sam's Announces Nationwide Recall of Two Varieties of Archer Farms Brand Cookies (January 23), U.S. Food & Drug Administration (FDA)
• Brent and Sam's Announces a Nationwide Recall of One Variety of Sam's Choice Brand Cookies (January 23), U.S. Food & Drug Administration (FDA)
• Amway Global Initiates Nationwide Recall of NUTRILITE Energy Bars Because of Possible Health Risk (January 23), U.S. Food & Drug Administration (FDA)
• Food Allergies: Reducing the Risks, U.S. Food & Drug Administration (FDA)
• FDA Web Page on Salmonella and Peanut Butter, U.S. Food & Drug Administration (FDA)
• Parker Products, Inc. Announces Nationwide Voluntary Recall of Certain Peanut Butter Products (January 22), U.S. Food & Drug Administration (FDA)
• Trader Joe's Announces Voluntary Recall of Trader Joe's Peanut Butter Chewy Coated and Drizzled Granola Bars, Nutty Chocolate Chewy Coated and Drizzled Granola Bars and Sutter's Formula Cookies Due to Possible Health Risk (January 22), U.S. Food & Drug Administration (FDA)
• Arbonne International Voluntarily Recalls Figure 8 Peanut Butter Chews Due To Possible Health Risk (January 22), U.S. Food & Drug Administration (FDA)
• Jimmy's Cookies Issues Nationwide Recall of Various Peanut Butter Cookies Due to Possible Health Risk (January 22), U.S. Food & Drug Administration (FDA)
• Perry's Ice Cream Company Adds Two Products to Voluntary Recall of Select Peanut Butter Ice Cream Products (January 22), U.S. Food & Drug Administration (FDA)
• Kroger Recalls Additional Select Ice Cream Product Due to Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• General Nutrition Centers, Inc. Announces Nationwide Voluntary Recall of Certain Lots of GNC Triflex Peanut Butter Soft Chews (January 22), U.S. Food & Drug Administration (FDA)
• Chef Jay's Food Products Announces Voluntary Nationwide Recall of Products Containing Peanut Butter Due to Possible Health Risk (January 21), U.S. Food & Drug Administration (FDA)
• Rain Creek Baking Corporation Announces Voluntary Withdrawal of Peanut Butter Turtles, Peanut Butter Baskets and Peanut Butter Princesses Due to Possible Health Risk (January 22), U.S. Food & Drug Administration (FDA)
• South Bend Chocolate Company Extends Nationwide Recall of Candy Containing Peanut Butter Because of Possible Salmonella Contamination (January 22), U.S. Food & Drug Administration (FDA)
• Nash Finch Recalls Bakery Products With Peanut Butter Distributed in Seven States Due to Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Aspen Hills, Inc. Announces Voluntary Product Recall of Certain Cookie Dough Products (January 22), U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Expands Peanut Butter Recall to Include Pet Food Products, U.S. Food & Drug Administration (FDA)
• Best Brands Corp. Announces Voluntary Recall of Peanut Butter Frozen Cookie Dough (January 21), U.S. Food & Drug Administration (FDA)
• Lovin Oven, LLC Announces Voluntary Nationwide Recall of Certain Health Valley Organic Peanut Crunch Chewy Granola Bars (January 21), U.S. Food & Drug Administration (FDA)
• Landies Candies Co. Inc Announces Voluntary Recall of Select Peanut Butter Filled Chocolates Due to Possible Health Risk (January 21), U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 21, 2009, U.S. Food & Drug Administration (FDA)
• Weis Markets Announces Voluntary Recall of Weis Quality (WQ) Cheese Peanut Butter Sandwich Crackers and WQ Toasted Peanut Butter Sandwich Crackers Due to Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Blanton's Candies Recalls Peanut Butter Sticks Because of Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Dinners Ready Meridian Recalls November and December Asian Marinated Flank Steak, Indonesian Chicken and Chicken Satay Prepared Meals Because of Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Boca Grande Foods Announces a Nationwide Recall of POCO PAC, and GRANDE GOURMET Peanut Butter Products Because of Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Premier Nutrition Announces Voluntary Nationwide Recall of selected TWISTED and TITAN Branded Bars Containing Peanut Butter Due to Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• NutriSystem Announces Nationwide Voluntary Recall of Peanut Butter Granola Bar Due to Possible Peanut Corporation of America (PCA) Contamination and Potential Health Risk (January 21), U.S. Food & Drug Administration (FDA)
• Ready Pac Foods, Inc Announces Voluntary Product Recall (January 20), U.S. Food & Drug Administration (FDA)
• PetSmart Voluntarily Recalls Grreat Choice Dog Biscuits (January 20), U.S. Food & Drug Administration (FDA)
• Nature's Path Recalls Peanut Butter Optimum Energy Bars Nationwide Because of Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Country Maid Announces Voluntary Nationwide Recall of Classic Breaks Peanut Butter Cookie Dough Due to Possible Health Risk (January 20), U.S. Food & Drug Administration (FDA)
• Evening Rise Bread Co. Recalls Peanut Butter Cookies and Bars Because of Possible Health Risk (January 19), U.S. Food & Drug Administration (FDA)
• Clif Bar and Company Announces Voluntary Nationwide Recall of CLIF and LUNA Branded Bars Containing Peanut Butter Due to Possible Health Risk (January 19), U.S. Food & Drug Administration (FDA)
• Kroger Recalls Select Ice Cream Products Due to Possible Health Risk (January 19), U.S. Food & Drug Administration (FDA)
• Abbott Nutrition Announces Voluntary Recall of ZonePerfect Chocolate Peanut Butter Bars, ZonePerfect Peanut Toffee Bars and NutriPals Peanut Butter Chocolate Bars in U.S., Mexico, New Zealand and Singapore (January 19), U.S. Food & Drug Administration (FDA)
• K-Fat Inc. Issues Alert on Uneviscerated Mackerel Fish (January 19), U.S. Food & Drug Administration (FDA)
• Meijer Announces Voluntary Recall for Some Meijer Brand Peanut Butter Crackers and Ice Cream Because of Possible Health Risk (January 19), U.S. Food & Drug Administration (FDA)
• Ralcorp Frozen Bakery Products Recalls Food Lion Bake Shop Peanut Butter Cookies Nationwide Because Of Possible Health Risk (January 18), U.S. Food & Drug Administration (FDA)
• Ralcorp Frozen Bakery Products Recalls Lofthouse Peanut Butter Cookies, Chuck's Chunky Peanut Butter Cookies And Pastries Plus Gourmet Cookies Nationwide Because Of Possible Health Risk (January 18), U.S. Food & Drug Administration (FDA)
• Ralcorp Frozen Bakery Products Recalls Wal-Mart Bakery Brand Peanut Butter Cookies Because Of Possible Health Risk (January 18), U.S. Food & Drug Administration (FDA)
• Peanut Corporation of America Expands Nationwide Recall of Peanut Butter (January 18), U.S. Food & Drug Administration (FDA)
• South Bend Chocolate Company Recalls Various Candys Containing Peanut Butter Because of Possible Salmonella Contamination (January 18), U.S. Food & Drug Administration (FDA)
• McKee Foods Corporation Announces Voluntary Nationwide Recall of Little Debbie Peanut Butter Toasty and Peanut Butter Cheese Sandwich Crackers Because of Possible Health Risk (January 18), U.S. Food & Drug Administration (FDA)
• Perry's Ice Cream Company Announces Voluntary Recall of Select Peanut Butter Ice Cream Products Due to Possible Health Risk (January 17), U.S. Food & Drug Administration (FDA)
• Hy-Vee Inc. Recalls Bakery Products With Peanut Butter Distributed in Seven States Due to Possible Health Risk (January 17), U.S. Food & Drug Administration (FDA)
• Peanut Corporation of America Expands Nationwide Recall of Peanut Butter (January 16), U.S. Food & Drug Administration (FDA)
• Kellogg Company Announces Voluntary Nationwide Recall of Austin and Keebler Branded Peanut Butter Sandwich Crackers and Select Snack-Size Packs of Famous Amos And Keebler Soft Batch Peanut Butter Cookies Because of Possible Health Risk (January 16), U.S. Food & Drug Administration (FDA)
• Salmonella recovered from King Nut peanut butter by MDA lab found to be a genetic match to cases in national Salmonella outbreak (January 12), U.S. Food & Drug Administration (FDA)
• Salmonella-Tainted Peanut Butter Found in Connecticut (January 16), U.S. Food & Drug Administration (FDA)
• FDA Approves RiaSTAP for Treatment of Bleeding in Patients with Rare Genetic Defect, U.S. Food & Drug Administration (FDA)
• FDA Alerts Public about Danger of Skin Numbing Products, U.S. Food & Drug Administration (FDA)
• MedWatch - Drug Safety Newsletter, Volume 2, Issue 1, 2009, U.S. Food & Drug Administration (FDA)
• MedWatch - Topical Anesthetics: Public Health Advisory issued regarding serious hazards of using skin numbing products, U.S. Food & Drug Administration (FDA)
• Final Guidance on Genetically Engineered Animals, U.S. Food & Drug Administration (FDA)
• FDA Issues Guidances for Industry to Improve the Safety of Food, Feed and Drugs, U.S. Food & Drug Administration (FDA)
• FDA Issues Final Guidance on Regulating Genetically Engineered Animals, U.S. Food & Drug Administration (FDA)
• Kellogg Company Announces Precautionary Hold on Austin and Keebler Branded Peanut Butter Sandwich Crackers (January 14), U.S. Food & Drug Administration (FDA)
• FDA Launches Pilot Program To Improve the Safety of Drugs and Active Drug Ingredients Produced Outside the United States, U.S. Food & Drug Administration (FDA)
• Peanut Corporation of America Announces Voluntary Nationwide Recall of Peanut Butter (January 13), U.S. Food & Drug Administration (FDA)
• Peanut Corporation of America Announces Voluntary Nationwide Recall of Peanut Butter (December 13), U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 14, 2009, U.S. Food & Drug Administration (FDA)
• MedWatch - Singulair (montelukast): updated information to March 2008 Early Communication, U.S. Food & Drug Administration (FDA)
• FDA Announces Two Appointments, U.S. Food & Drug Administration (FDA)
• Federal Agencies Issue Draft Guidance for Industry Good Importer Practices, U.S. Food & Drug Administration (FDA)
• Domega International Ltd., Inc Issues An Alert On Undeclared Sulfites In Guangdayuan Brand Dried Sweet Potato (December 31), U.S. Food & Drug Administration (FDA)
• Cafe Favorites Issues a Recall of Sandwiches because of Possible Health Risks (January 10), U.S. Food & Drug Administration (FDA)
• Triple B Corporation dba S.T. Produce Issues Allergy Alert on Undeclared Allergens Walnuts and Almonds in Parfait Products (January 9), U.S. Food & Drug Administration (FDA)
• King Nut Issues Peanut Butter Recall (January 10), U.S. Food & Drug Administration (FDA)
• Understanding Antidepressant Medications, U.S. Food & Drug Administration (FDA)
• FDA Awaits Court's Entry of A Permanent Injunction Against Actavis Totowa, LLC, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ezetimibe/Simvastatin - Update of Safety Review, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January/February 2009 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 7, 2009, U.S. Food & Drug Administration (FDA)
• Celeste Industries Corporation Recalls All Lots of simplySmart Remove Make Up Remover (January 5), U.S. Food & Drug Administration (FDA)
• National Brands Inc. Issues a Nationwide Recall of Topaz brand Wafer Rolls Because of Possible Health Risks (December 19), U.S. Food & Drug Administration (FDA)
• FDA Announces Class I Recall of Ophthalmic Surgical Device, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Announces Class I Recall of Ophthalmic Surgical Device, U.S. Food & Drug Administration (FDA)
• FDA Prevents Two Dairies from Adulterating Animal Drugs and Food, U.S. Food & Drug Administration (FDA)
• Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile (December 23), U.S. Food & Drug Administration (FDA)
• MedWatch - Innohep (tinzaparin sodium) Dear Healthcare Professional Letter issued re: increased risk of death in renal impaired elderly, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 31, 2008, U.S. Food & Drug Administration (FDA)
• FDA Approves First Nucleic Acid Test to Screen for Additional Types of HIV in Donated Blood and Tissue, U.S. Food & Drug Administration (FDA)
• Tainted Weight Loss Pills Flagged as Health Risks, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Tainted Weight Loss Pills Flagged as Health Risks, U.S. Food & Drug Administration (FDA)
• FDA Approves Drug for Patients with Advanced Prostate Cancer, U.S. Food & Drug Administration (FDA)
• KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23), U.S. Food & Drug Administration (FDA)
• MedWatch - Stryker Custom Cranial Implant Kits: Class 1 recall due to lack of assurance of sterility and risk on infection, U.S. Food & Drug Administration (FDA)
• FDA Approves First Imaging Agent to Enhance Scans of Blood Flow, U.S. Food & Drug Administration (FDA)
• MedWatch - Hydromorphone tablets [ETHEX] recalled due to oversided tablets and potential for over dosage, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 24, 2008, U.S. Food & Drug Administration (FDA)
• Caution to Dog Owners About Chicken Jerky Products, U.S. Food & Drug Administration (FDA)
• ETHEX Corporation Initiated Nationwide Voluntary Recall of a Single Lot of Hydromorphone HCl 2 mg Tablets Due to Potential for Oversized Tablet (December 23), U.S. Food & Drug Administration (FDA)
• KV Pharmaceutical Voluntarily Suspends All Shipments of its Approved Tablet-form Drugs (December 23), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Weight Loss Pills contain undeclared, active pharmaceutical ingredients that may put consumers' health at risk, U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers About Tainted Weight Loss Pills (December 22), U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers About Tainted Weight Loss Pills, U.S. Food & Drug Administration (FDA)
• FDA Obtains Injunction to Stop Production of Illegally Medicated Animal Feed, U.S. Food & Drug Administration (FDA)
• Dorsey Marketing Inc. Voluntarily Recalls Three G and J Gourmet Market Cocoa Products: 120126, 120129, 120144 (December 19), U.S. Food & Drug Administration (FDA)
• FDA Approves Gleevec to Prevent Recurrence of Rare Gastrointestinal Cancer, U.S. Food & Drug Administration (FDA)
• MedWatch - SunMed Greenline/D MacIntosh No. 3 Laryngoscope Blades recalled due to potential to break during use, U.S. Food & Drug Administration (FDA)
• Preliminary Animal Health Notification - Chicken Jerky Products for Dogs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - October 2008 Drug Safety Labeling Changes for 61 Drugs Now Available on Web, U.S. Food & Drug Administration (FDA)
• Interfood Shareholding Company Issues a Nationwide recall of Wonderfarm Brand Biscuits Because of Possible Health Risk (December 9), U.S. Food & Drug Administration (FDA)
• Historic Building One Dedicated at FDA?s White Oak Federal Research Center, U.S. Food & Drug Administration (FDA)
• FDA Approves Drug that Boosts Stem Cell Yield for Bone Marrow Transplants, U.S. Food & Drug Administration (FDA)
• FDA Announces New Recommendations on Evaluating Cardiovascular Risk in Drugs Intended to Treat Type 2 Diabetes, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 17, 2008, U.S. Food & Drug Administration (FDA)
• FDA Requires Warnings about Risk of Suicidal Thoughts and Behavior for Antiepileptic Medications, U.S. Food & Drug Administration (FDA)
• Botulism Risk From Ungutted, Salt-Cured Alewives Fish, U.S. Food & Drug Administration (FDA)
• Prescription Drug Leaflets Need Improvement, U.S. Food & Drug Administration (FDA)
• Study Finds Much of Private-Sector Consumer Medication Information Not Consistently Useful, U.S. Food & Drug Administration (FDA)
• Kidney Risk Spurs Warning on Bowel Cleansers, U.S. Food & Drug Administration (FDA)
• FDA Announces Class I Recalls of Two Unapproved Devices (December 15), U.S. Food & Drug Administration (FDA)
• FDA Announces Class I Recalls of Two Unapproved Devices, U.S. Food & Drug Administration (FDA)
• Kashi Company Issues Allergy Alert on Undeclared Milk in Kashi GOLEAN® Powder Chocolate Energy Shake Mix (December 13), U.S. Food & Drug Administration (FDA)
• Urgent: Food Product Recall Re: Imitation Cream Cheese and Low Protein Peanot Butter(December 11), U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers and Retailers of Botulism Risk from Ungutted, Salt-Cured Alewives (Gaspereaux) Fish (December 12), U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers and Retailers of Botulism Risk from Ungutted, Salt-Cured Alewives (Gaspereaux) Fish, U.S. Food & Drug Administration (FDA)
• Get Set for Winter Illness Season, U.S. Food & Drug Administration (FDA)
• Some Medications and Driving Don't Mix, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Oral Sodium Phosphate (OSP) Products for Bowel Cleansing: reports of acute phosphate nephropathy, Boxed Warning to be added to labeling, U.S. Food & Drug Administration (FDA)
• FDA Requires New Safety Measures for Oral Sodium Phosphate Products to Reduce Risk of Acute Kidney Injury, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Gravity Compensating Accessory by Integra NeuroSciences: recalled because devices may leak cerebrospinal fluid, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Healon D Ophthalmic Viscosurgical Device: recall due to syringes with endotoxin levels above the required limit, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 10, 2008, U.S. Food & Drug Administration (FDA)
• FDA Education Program Wins Award, U.S. Food & Drug Administration (FDA)
• FDA Beyond Our Borders, U.S. Food & Drug Administration (FDA)
• FDA Announces Permanent Injunction Against Wilderness Family Naturals LLC, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 20 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP: Recall of one lot due to possible incorrect bar code for 5% Dextrose Injection, USP., U.S. Food & Drug Administration (FDA)
• Hospira Issues Voluntary Recall of One Lot of 20meq Potassium Chloride in 5 Percent Dextrose and 0.45 Percent Sodium Chloride Injection, USP Due to Incorrect Bar Code Label (December 8), U.S. Food & Drug Administration (FDA)
• Balanced Health Products, Inc. Expands Voluntary Urgent Nationwide Recall of Starcaps Dietary Supplement Capsules Found to Contain an Undeclared Drug Ingredient (December 8), U.S. Food & Drug Administration (FDA)
• FDA MedWatch-Terumo Cardiovascular Systems Tenderflow Pediatric Arterial Cannulae- Recalled due to reports of difficulty retracting the introducer from the cannula, U.S. Food & Drug Administration (FDA)
• Terumo Cardiovascular Systems Issues Urgent, Nationwide/Worldwide Recall of Pediatric Arterial Cannulae (December 8), U.S. Food & Drug Administration (FDA)
• Louisiana Fish Fry Products Issues Nationwide Allergy Alert on Undeclared Buttermilk in Chicken and Fish Bake Seasoned Coating Mix (December 5), U.S. Food & Drug Administration (FDA)
• Walgreens Recalls 173 Teddy Bears With Chocolate Bars Sold Since Late September 2008 (December 5), U.S. Food & Drug Administration (FDA)
• Mom's Food Products, Inc. Issues Allergy Alert On Undeclared Eggs In Pimento Spread Sandwiches (December 2), U.S. Food & Drug Administration (FDA)
• Limited Recall of LAND O LAKES Sheep Balancer B136 (December 4), U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 03, 2008, U.S. Food & Drug Administration (FDA)
• FDA, EPA and USDA Conclude That Accidental Release of Genetically Engineered Cotton Poses No Safety Risk to Humans or Animals, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Teams With WebMD For New Online Consumer Health Information, U.S. Food & Drug Administration (FDA)
• FDA Announces Participants of Pilot Program for Third-Party Certification of Imported Aquacultured Shrimp, U.S. Food & Drug Administration (FDA)
• FDA Partners With WebMD to Better Serve Consumers, U.S. Food & Drug Administration (FDA)
• FDA Teams With WebMD For New Online Consumer Health Information, U.S. Food & Drug Administration (FDA)
• MedWatch - Innohep (tinzaparin): Clinical study stopped early because of interim finding of increased all-cause mortality in patients who received drug, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - The December 2008 Patient Safety News Is Now Available..., U.S. Food & Drug Administration (FDA)
• FDA Reports Significant Progress in Protecting the Food Supply, U.S. Food & Drug Administration (FDA)
• FDA Acts to Reduce Risk of Salmonella Infections, U.S. Food & Drug Administration (FDA)
• Avoiding Drug Interactions, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 26, 2008, U.S. Food & Drug Administration (FDA)
• MedWatch - Zhen De Shou Fat Loss Capsules recalled due to undeclared drug, sibutramine which may cause significant increase in blood pressure, U.S. Food & Drug Administration (FDA)
• MedWatch - Starcaps Dietary Supplement Capsules - Recall due to undeclared drug, Bumetanide, resulting in drug interactions, hypotension, U.S. Food & Drug Administration (FDA)
• Balanced Health Products, Inc. Conducts Voluntary Urgent Nationwide Recall of Starcaps Dietary Supplement Capsules Found to Contain an Undeclared Drug Ingredient (November 24), U.S. Food & Drug Administration (FDA)
• Fashion Sanctuary Issues a Voluntary Nationwide Recall of All Lots of Zhen De Shou Fat Loss Capsules Found to Contain an Undeclared Drug Ingredient (November 23), U.S. Food & Drug Administration (FDA)
• Stop and Shop Recalls Butternut Squash in Prepared Turkey and Ham Dinner (November 24), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Phenytoin and Fosphenytoin Sodium associated with potential increased risk of serious skin reactions, U.S. Food & Drug Administration (FDA)
• FDA Approves New Drug to Alleviate Moderate to Severe Pain, U.S. Food & Drug Administration (FDA)
• MedWatch - Animas Insulin Pumps: Battery Caps - Class 1 recall due to inadvertent device resetting, risk of hyperglycemia, U.S. Food & Drug Administration (FDA)
• PANOS Brands Recalls Vegan Rella Cheddar Block (November 21), U.S. Food & Drug Administration (FDA)
• FDA Acts to Avoid Shortage and Strengthen the Safety of Sucraid, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets, Inc. Issues Voluntary Recall on Wegmans Italian Classics Seasoned Tomato Sauce (November 20), U.S. Food & Drug Administration (FDA)
• FDA Approves New Drug to Treat Severe Form of Epilepsy, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 19, 2008, U.S. Food & Drug Administration (FDA)
• FDA MedWatch: Benzoyl Peroxide Acne Cream 10%: Product Recalled Because Samples Contained Burkholderia Cepacia Bacteria, U.S. Food & Drug Administration (FDA)
• Beware of Extortion Scam by FDA Impersonators, U.S. Food & Drug Administration (FDA)
• Seattle's Favorite Gourmet Cookies and Dessert Co Issues Nationwide Allergy Alert on Undeclared Milk in Muffin Tops (November 14), U.S. Food & Drug Administration (FDA)
• CSI USA, Inc. Issues Voluntary National Recall of Topical Acne Cream (November 13), U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 12, 2008, U.S. Food & Drug Administration (FDA)
• FDA Warns Public of Extortion Scam by FDA Impersonators, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Bisphosphonates-Update To The Early Communication Issued Regarding Atrial Fibrillation With Bisphosphonates, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- FDA MedWatch- Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas)- Product Recalled Due To Possible Metal Fragments In The Bottle, U.S. Food & Drug Administration (FDA)
• Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments (November 7), U.S. Food & Drug Administration (FDA)
• Amy's Kitchen Inc. Issues Allergy Alert and Voluntary National Recall due to Possible Undeclared Milk in Tofu Scramble in a Pocket Sandwich; Lot Code H148 (November 7), U.S. Food & Drug Administration (FDA)
• Nestle Withdraws Nestle Farinha Lactea Cereal in the United States (November 3), U.S. Food & Drug Administration (FDA)
• FDA MedWatch- FDA MedWatch- Propafenone HCl, Isosorbide Mononitrate Extended Release, Morphine Sulfate Immediate and Extended Release, Dextroamphetamine Sulfate- Products Recalled Due To The Potential For Oversized Tablets, U.S. Food & Drug Administration (FDA)
• ETHEX Corporation Initiated Nationwide Voluntary Recalls of Specific Lots of Five Generic Products Due to the Potential for Oversized Tablets (November 7), U.S. Food & Drug Administration (FDA)
• Nestle USA Voluntarily Recalls Two Production Codes of Nestle Nesquik Strawberry Powder (November 7), U.S. Food & Drug Administration (FDA)
• MedWatch - WalMart "ReliOn" insulin syringe recall due to potential for serious overdose, U.S. Food & Drug Administration (FDA)
• FDA Seizes Contaminated Heparin from a Cincinnati Manufacturer, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 5, 2008, U.S. Food & Drug Administration (FDA)
• FDA Reports Nationwide Recall of Mislabeled ReliOn Insulin Syringes (November 5), U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Reports Nationwide Recall of Mislabeled ReliOn Insulin Syringes (November 5), U.S. Food & Drug Administration (FDA)
• Food Safety Tips for Healthy Holidays, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Food Safety Tips for Healthy Holidays, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - September 2008 Drug Safety-Related Labeling Changes for 36 Drugs Now Available on Web, U.S. Food & Drug Administration (FDA)
• General Mills Issues Voluntary Class One Recall Involving One Day's Production of Progresso Hearty Tomato Soup (October 31), U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator- Class I Recall Because Of Unsupported Claims, U.S. Food & Drug Administration (FDA)
• Everlasting Distributors Inc. Issues a Nationwide Recall of Fresh and Crispy Jacobina Biscuits Because of Possible Health Risks (October 29), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - The November 2008 Patient Safety News Is Now Available..., U.S. Food & Drug Administration (FDA)
• FDA Approves Toviaz, a New Drug to Treat Overactive Bladder, U.S. Food & Drug Administration (FDA)
• HHS/FDA Grants Tentative Approval for 75th Generic Anti-Retroviral Drug as Part of President's Emergency Plan for AIDS Relief, U.S. Food & Drug Administration (FDA)
• Mexican Vanilla With Coumarin: No Bargain, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 29, 2008, U.S. Food & Drug Administration (FDA)
• FDA Statement on Release of Bisphenol A (BPA) Subcommittee Report, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Thoratec HeartMate II Left Ventricular Assist System- Device Correction: Wear And Fatigue Of The Percutaneous Lead Connecting The Blood Pump With The System Controller May Cause Serious Injury Or Death, U.S. Food & Drug Administration (FDA)
• FDA Warns Bayer About Two Unapproved Aspirin Products, U.S. Food & Drug Administration (FDA)
• FDA Issues Warning Letters to Bayer HealthCare for Illegally Marketing Two Unapproved Drugs, U.S. Food & Drug Administration (FDA)
• Mars Petcare US Issues Voluntary Recall of a Limited Number of Bags of SPECIAL KITTY Gourmet Sold at Wal-Mart locations in Fifteen States due to Potential Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Thoratec Corporation Issues Worldwide Medical Device Correction of HeartMate II Left Ventricular Assist System (October 24), U.S. Food & Drug Administration (FDA)
• FDA Approves Lung Valve to Control Some Air Leaks after Surgery, U.S. Food & Drug Administration (FDA)
• Portland Shellfish Co. Inc, Recalls Claw Island Brand Lobster Claw and Knuckle Meat Because of Possible Health Risk (October 21), U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 22, 2008, U.S. Food & Drug Administration (FDA)
• Nonna's Real Italiana Cuccine Issues an Allergy Alert on Undeclared Milk, Soy, and Wheat in Stuffed Artichokes (October 22), U.S. Food & Drug Administration (FDA)
• Harry and David Issues Nationwide Allergy Alert on Undeclared Pecans in Harry and David Moose Munch Confection, Milk Chocolate Gingerbread (October 22), U.S. Food & Drug Administration (FDA)
• Using Over-the-Counter Cough and Cold Products in Children, U.S. Food & Drug Administration (FDA)
• FDA MedWatch: Transvaginal Placement of Surgical Mesh- Serious Complications Associated With Transvaginal Placement Of Surgical Mesh In Repair of Pelvic Organ Prolapse And Stress Urinary Incontinence, U.S. Food & Drug Administration (FDA)
• The Hartz Mountain Corporation Voluntarily Recalls One Specific Lot of Nationwide Chicken-Basted Rawhide Chips Because of Possible Health Risk (October 20), U.S. Food & Drug Administration (FDA)
• Safety Concerns and Labeling Changes for Psoriasis Drug Raptiva, U.S. Food & Drug Administration (FDA)
• Lotte USA, Inc. Initiates Nationwide Recall of Koala's March Creme filled Cookies, U.S. Food & Drug Administration (FDA)
• MedWatch - Raptiva (efalizumab): Boxed Warning describes risk for life-threatening infections, U.S. Food & Drug Administration (FDA)
• FDA Approves Updated Labeling for Psoriasis Drug Raptiva, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Dextroamphetamine Sulfate 5mg Tablets- Drug Recall Due To The Potential For Oversized Tablets, U.S. Food & Drug Administration (FDA)
• Use Caution With Ayurvedic Products, U.S. Food & Drug Administration (FDA)
• Improper Use of Decorative Contacts May Haunt You, U.S. Food & Drug Administration (FDA)
• ETHEX Corporation Voluntarily Recalls Three Lots of Dextroamphetamine Sulfate 5mg Tablets Due to the Potential for Oversized Tablets (October 15), U.S. Food & Drug Administration (FDA)
• FDA Creates Web Page with Drug Safety Information for Patients, Health Care Professionals, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 15, 2008, U.S. Food & Drug Administration (FDA)
• JFC International, Inc. Issues Allergy Alert on Undeclared Sulfite in "Kyosai Sengiri Daikon" Dried Radish (October 10), U.S. Food & Drug Administration (FDA)
• Barry Callebaut USA LLC Issues Allergen Alert on Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips (October 10), U.S. Food & Drug Administration (FDA)
• HUA XIA Food Trade USA, Inc. Recalls YILI Brand Sour Milk Drink and YILI Brand Pure Milk Drink, Because of Possible Health Risk (October 10), U.S. Food & Drug Administration (FDA)
• FDA Licenses for Marketing New Therapy for Rare Genetic Disease, U.S. Food & Drug Administration (FDA)
• FDA Approves Rapaflo for the Treatment of Symptoms Due to an Enlarged Prostate Gland, U.S. Food & Drug Administration (FDA)
• FDA Launches Food Defense Awareness Training Kit for Employees in the Food Industry, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 8, 2008, U.S. Food & Drug Administration (FDA)
• FDA Licenses Drug to Prevent Joint Damage in Children with Hemophilia A, U.S. Food & Drug Administration (FDA)
• Russell Stover Candies, Inc. Issues Hazelnut Allergy Alert for the 2 7/8 Oz Size Of Private Reserve Assorted Chocolates (October 9), U.S. Food & Drug Administration (FDA)
• FDA MedWatch- OTC Cough and Cold Medicines- Product Labels Being Modified To State " Do Not Use" In Children Under 4 Years Of Age, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Statement Following CHPA's Announcement on Nonprescription Over-the-Counter Cough and Cold Medicines in Children, U.S. Food & Drug Administration (FDA)
• Recalls and Melamine Contamination, U.S. Food & Drug Administration (FDA)
• Consumer Alert: Undeclared Sulfites in Shad Raisins (October 6), U.S. Food & Drug Administration (FDA)
• Arnold Foods Company, Inc. Issues Allergy Alert on Undeclared Nuts in Brownberry Whole Grains Bread 100 Percent Whole Wheat (October 8), U.S. Food & Drug Administration (FDA)
• Consumer Alert: Possible Botulism Contamination in Frozen Salted Croaker (October 6), U.S. Food & Drug Administration (FDA)
• FDA Statement Following CHPA's Announcement on Nonprescription Over-the-Counter Cough and Cold Medicines in Children, U.S. Food & Drug Administration (FDA)
• FDA Approves Use of Temporary Pump to Assist Heart's Right Side, U.S. Food & Drug Administration (FDA)
• MedWatch - Tiotropium (Spiriva): updated information on risk of stroke and reports of cardiovascular adverse outcomes, U.S. Food & Drug Administration (FDA)
• FDA and PATH Malaria Vaccine Initiative Announce Research Collaboration, U.S. Food & Drug Administration (FDA)
• FDA Detects Melamine Contamination in Flavored Drink, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Detects Melamine Contamination in Flavored Drink, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces Availability of Revised 356v Form, U.S. Food & Drug Administration (FDA)
• McCormick and Company Has Recalled McCormick Enchilada Sauce Mix Due To Unlabeled Milk Ingredients (September 30), U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Nebion HLX-8 Magnetic Resonance Device: Device Not Approved By FDA, U.S. Food & Drug Administration (FDA)
• Tristar Food Wholesale Co Inc. Issues a Nationwide recall of Blue Cat Flavor Drink Because of Possible Health Risk (October 3), U.S. Food & Drug Administration (FDA)
• FDA Issues Interim Safety and Risk Assessment of Melamine and Melamine-related Compounds in Food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch- Medtronic Neuromodulation INDURA One-Piece Intrathecal Catheters, Sutureless Pump Connector Revision Kit, and Intrathecal Catheter Pump Segment Revision Kit- Class I Recall, U.S. Food & Drug Administration (FDA)
• Lion Pavilion Issues Alert on Undeclared Sulfites in Yulanpian Brand Dried Slices of Tender Bamboo Shoots (September 26), U.S. Food & Drug Administration (FDA)
• Mr. Brown 3-In-1 and and 2-In-1 Powdered Packets in Bag Coffee Mixes Due To Health Risk (October 1), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - The October 2008 FDA Patient Safety News Video is now available..., U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 1, 2008, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Launches New Public-access Database of Animal Drug Approvals, U.S. Food & Drug Administration (FDA)
• FDA Awards $5.2 Million in Grants to Further Food and Feed Safety, U.S. Food & Drug Administration (FDA)
• FDA Awards up to $2.5 Billion to Modernize Information Technology over Ten Years, U.S. Food & Drug Administration (FDA)
• NY Fish Inc. Recalls Imperial-European Style Smoked Salmon Because of Possible Health Risk (September 26), U.S. Food & Drug Administration (FDA)
• Keeping Watch Over Direct-to-Consumer Ads, U.S. Food & Drug Administration (FDA)
• Is It Really FDA Approved?, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Statin drugs and risk of amyotrophic lateral sclerosis (ALS), U.S. Food & Drug Administration (FDA)
• FDA Analysis Shows Cholesterol Lowering Medications Do Not Increase the Risk of Lou Gehrig's Disease, U.S. Food & Drug Administration (FDA)
• Addressing Questions About Gardasil, U.S. Food & Drug Administration (FDA)
• QFCO, Inc. Recalls White Rabbit Candy Because of Possible Health Risk (September 26), U.S. Food & Drug Administration (FDA)
• Vaccines Stand Ready for Flu Season, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Epoetin alfa- Preliminary Safety Findings Show More Deaths In Patients Given Epoetin-alpha Versus Placebo, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 24, 2008, U.S. Food & Drug Administration (FDA)
• CaJohns Fiery Foods Company Recalls HDH Grillin' Sauce (September 24), U.S. Food & Drug Administration (FDA)
• Mom's Food Products, Inc. Issues Allergy Alert On Undeclared Eggs in Sandwiches and Potato Salad (September 23), U.S. Food & Drug Administration (FDA)
• Fineland Corp Issues Alert on Undeclared Sulfites in Ying Feng Foodstuffs Brand Pumpkin Seeds (September 23), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ammonul (sodium phenylacetate and sodium benzoate) Injection 10%/10% - Particulate matter detected in product, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tarceva (erlotinib) - Cases of hepatic failure and hepatorenal syndrome, including fatalities, have been reported during use of Tarceva, U.S. Food & Drug Administration (FDA)
• FDA Warns Companies to Stop Marketing Unapproved Ophthalmic Balanced Salt Solution Drug Products and Topical Drug Products Containing Papain, U.S. Food & Drug Administration (FDA)
• FDA Updates Health Information Advisory on Melamine Contamination, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Updates Health Information Advisory on Melamine Contamination, U.S. Food & Drug Administration (FDA)
  • FDA Updates Health Information Advisory on Melamine Contamination, U.S. Food & Drug Administration (FDA)
• Derringer Foodservices Issues Allergy Alert on Albacore Tuna Salad Hoagie (September 17), U.S. Food & Drug Administration (FDA)
• K-Fat Inc. Issues Alert On Undeclared Sulfites In "Mut Gung Sweetened Ginger" (September 18), U.S. Food & Drug Administration (FDA)
• FDA MedWatch- FDA Drug Safety Newsletter- Summer 2008 Edition Available For Healthcare Professionals And The Medical Community, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Phosphocol P 32- Risk Of Leukemia Associated With Off-Label Intra-articular Use In Children, U.S. Food & Drug Administration (FDA)
• Draft Guidance on Genetically Engineered Animals, U.S. Food & Drug Administration (FDA)
• FDA Proposes Label Requirements for Refused Imported Foods, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 17, 2008, U.S. Food & Drug Administration (FDA)
• FDA Issues Draft Guidance on Regulating Genetically Engineered Animals, U.S. Food & Drug Administration (FDA)
• Bimbo Bakeries USA Issues an Allergy Alert on Undeclared Tree Nuts in Oroweat 100 Percent Whole Wheat Bread Packaging (September 16), U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Issues Warning Letters to Ranbaxy Laboratories Ltd., and an Import Alert for Drugs from Two Ranbaxy Plants in India, U.S. Food & Drug Administration (FDA)
• FDA Issues Warning Letters to Ranbaxy Laboratories Ltd., and an Import Alert for Drugs from Two Ranbaxy Plants in India, U.S. Food & Drug Administration (FDA)
• In-Body Pediatric Devices Pose Unique Challenges, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - August 2008 Drug Safety-Related Labeling Changes for 41 Drugs Now Available on Web, U.S. Food & Drug Administration (FDA)
• Ralston Foods Issues Allergy Alert For Undeclared Milk Ingredients In Western Family Variety Pack Instant Oatmeal (September 15), U.S. Food & Drug Administration (FDA)
• Allergy Alert on Undeclared Dairy in Margaritaville Island Lime Tortilla Chips (September 12), U.S. Food & Drug Administration (FDA)
• Wegmans Expands Dates of Bagel Recall and Includes Additional Bakery Products (September 11), U.S. Food & Drug Administration (FDA)
• FDA Requires Stronger Fungal Infection Warning for TNF Blockers, U.S. Food & Drug Administration (FDA)
• Health Information Advisory on Infant Formula, U.S. Food & Drug Administration (FDA)
• FDA News Digest for August 18, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for August 11, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for July 28, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for July 15, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for July 7, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for June 9, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for June 2, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for May 27, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for May 19, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for May 12, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for May 5, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for April 28, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for April 7, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for March 31, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
  • FDA News Digest, U.S. Food & Drug Administration (FDA)
• FDA News Digest for March 18, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for March 10, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for March 3, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for February 25, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for February 19, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for February 11, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for February 4, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for January 28, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for January 22, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for January 14, 2008, U.S. Food & Drug Administration (FDA)
• FDA News Digest for January 7, 2007, U.S. Food & Drug Administration (FDA)
• FDA News Digest for December 18, 2007, U.S. Food & Drug Administration (FDA)
• FDA News Digest for December 10, 2007, U.S. Food & Drug Administration (FDA)
• FDA News Digest for December 3, 2007, U.S. Food & Drug Administration (FDA)
• FDA News Digest for November 26, 2007, U.S. Food & Drug Administration (FDA)
• FDA News Digest for November 19, 2007, U.S. Food & Drug Administration (FDA)
• FDA News Digest for November 13, 2007, FDA News Digest
• Notice to FDA News Digest subscribers, FDA News Digest
• FDA News Digest for November 5, 2007, FDA News Digest
• FDA News Digest for October 9, 2007, FDA News Digest
• FDA News Digest for October 1, 2007, FDA News Digest
• FDA News Digest for September 24, 2007, FDA News Digest
• FDA News Digest for September 17, 2007, FDA News Digest
• FDA News Digest for September 10, 2007, FDA News Digest
• FDA News Digest for September 4, 2007 (resend due to non-functioning link), FDA News Digest
• FDA News Digest for August 27, 2007, FDA News Digest
• FDA News Digest for August 20, 2007, FDA News Digest
• FDA News Digest for August 13, 2007, FDA News Digest
• FDA News Digest for August 6, 2007, FDA News Digest
• FDA News Digest for July 30, 2007, FDA News Digest
• FDA News Digest for July 23, 2007, FDA News Digest
• FDA News Digest for July 16, 2007, FDA News Digest
• FDA News Digest for July 9, 2007, FDA News Digest
• FDA News Digest for July 2, 2007, FDA News Digest
• FDA News Digest for June 25, 2007, FDA News Digest
• FDA News Digest for June 18, 2007, FDA News Digest
• FDA News Digest for June 11, 2007, FDA News Digest
• FDA News Digest for June 4, 2007, FDA News Digest
• FDA News Digest for May 29, 2007, FDA News Digest
• FDA News Digest for May 21, 2007, FDA News Digest
• FDA News Digest for May 14, 2007, FDA News Digest
• FDA News Digest for May 7, 2007, FDA News Digest
• FDA News Digest for April 30, 2007, FDA News Digest
• FDA News Digest for April 23, 2007, FDA News Digest
• FDA News Digest for April 16, 2007, FDA News Digest
• FDA News Digest for April 9, 2007, FDA News Digest
• FDA News Digest for April 2, 2007, FDA News Digest
• This week's News Digest draft, FDA News Digest
• FDA News Digest for March 19, 2007, FDA News Digest
• FDA News Digest for March 12, 2007, FDA News Digest
• FDA News Digest for March 5, 2007, FDA News Digest
• FDA News Digest for February 26, 2007, FDA News Digest
• FDA News Digest for February 20, 2007, FDA News Digest
• FDA News Digest for February 12, 2007, FDA News Digest
• FDA News Digest for February 5, 2007, FDA News Digest
• FDA News Digest for January 29, 2007, FDA News Digest
• FDA News Digest for January 22, 2007, FDA News Digest
• FDA News Digest for January 16, 2007, FDA News Digest
• FDA News Digest for January 8, 2007, FDA News Digest
• FDA News Digest for January 3, 2007, FDA News Digest
• FDA News Digest for December 18, 2006, FDA News Digest
• FDA News Digest for December 11, 2006, FDA News Digest
• FDA News Digest for December 4, 2006, FDA News Digest
• FDA News Digest for November 27, 2006, FDA News Digest
• FDA News Digest for November 20, 2006, FDA News Digest
• FDA News Digest for November 13, 2006, FDA News Digest
• FDA News Digest for November 6, 2006, FDA News Digest
• FDA News Digest for October 30, 2006, FDA News Digest
• FDA News Digest for October 23, 2006, FDA News Digest
• FDA News Digest for October 16, 2006, FDA News Digest
• FDA News Digest for October 10, 2006, FDA News Digest
• FDA News Digest for October 2, 2006, FDA News Digest
• FDA News Digest for September 25, 2006, FDA News Digest
• FDA News Digest for September 18, 2006, FDA News Digest
• FDA News Digest for September 11, 2006, FDA News Digest
• FDA News Digest for September 5, 2006, FDA News Digest
• FDA News Digest for August 28, 2006, FDA News Digest
• FDA News Digest for August 21, 2006, FDA News Digest
• FDA News Digest for August 14, 2006, FDA News Digest
• FDA News Digest for August 7, 2006, FDA News Digest
• FDA News Digest for July 31, 2006, FDA News Digest
• FDA News Digest for July 24, 2006, FDA News Digest
• FDA News Digest for July 17, 2006, FDA News Digest
• FDA News Digest for July 10, 2006, FDA News Digest
• FDA News Digest for July 3, 2006, FDA News Digest
• FDA News Digest for June 26, 2006, FDA News Digest
• FDA News Digest for June 19, 2006, FDA News Digest
• FDA News Digest for June 12, 2006, FDA News Digest
• FDA News Digest for June 5, 2006, FDA News Digest
• FDA News Digest for May 30, 2006, FDA News Digest
• FDA News Digest for May 22, 2006, FDA News Digest
• FDA News Digest for May 15, 2006, FDA News Digest
• FDA News Digest for May 8, 2006, FDA News Digest
• FDA News Digest for May 1, 2006, FDA News Digest
• FDA News Digest for April 24, 2006, FDA News Digest
• FDA News Digest for April 17, 2006, FDA News Digest
• FDA News Digest for April 10, 2006, FDA News Digest
• FDA News Digest for April 3, 2006, FDA News Digest
• FDA News Digest for March 27, 2006, FDA News Digest
• FDA News Digest for March 20, 2006, FDA News Digest
• FDA News Digest for March 13, 2006, FDA News Digest
• FDA News Digest for March 6, 2006, FDA News Digest
• FDA News Digest for February 27, 2006, FDA News Digest
• FDA News Digest for February 21, 2006, FDA News Digest
• FDA News Digest for February 13, 2006, FDA News Digest
• FDA News Digest for February 6, 2006, FDA News Digest
• FDA News Digest for January 30, 2006, FDA News Digest
• FDA News Digest for January 23, 2006, FDA News Digest
• FDA News Digest for January 17, 2006, FDA News Digest
• FDA News Digest for January 9, 2006, FDA News Digest
• FDA News Digest for January 3, 2006, FDA News Digest
• FDA News Digest for December 19, 2005, FDA News Digest
• FDA News Digest for December 12, 2005, FDA News Digest
• FDA News Digest for December 5, 2005, FDA News Digest
• FDA News Digest for November 28, 2005, FDA News Digest
• FDA News Digest for November 21, 2005, FDA News Digest
• FDA News Digest for November 14, 2005, FDA News Digest
• FDA News Digest for November 7, 2005, FDA News Digest
• FDA News Digest for October 31, 2005, FDA News Digest
• FDA News Digest for October 24, 2005, FDA News Digest
• FDA News Digest for October 17, 2005, FDA News Digest
• FDA News Digest for October 11, 2005, FDA News Digest
• FDA News Digest for October 3, 2005, FDA News Digest
• FDA News Digest for September 26, 2005, FDA News Digest
• FDA News Digest for September 19, 2005, FDA News Digest
• FDA News Digest for September 12, 2005, FDA News Digest
• FDA News Digest for September 6, 2005, FDA News Digest
• FDA News Digest for August 29, 2005, FDA News Digest
• FDA News Digest for August 22, 2005, FDA News Digest
• FDA News Digest for August 15, 2005, FDA News Digest
• FDA News Digest for August 8, 2005, FDA News Digest
• FDA News Digest for August 1, 2005, FDA News Digest
• FDA News Digest for July 25, 2005, FDA News Digest
• FDA News Digest for July 18, 2005, FDA News Digest
• FDA News Digest for July 11, 2005, FDA News Digest
• FDA News Digest for July 5, 2005, FDA News Digest
• FDA News Digest for June 27, 2005, FDA News Digest
• FDA News Digest for June 20, 2005, FDA News Digest
• FDA News Digest for June 13, 2005, FDA News Digest
• FDA News Digest for June 6, 2005, FDA News Digest
• FDA News Digest for May 31, 2005, FDA News Digest
• FDA News Digest for May 23, 2005, FDA News Digest
• FDA News Digest for May 16, 2005, FDA News Digest
• FDA News Digest for May 9, 2005, FDA News Digest
• FDA News Digest for May 2, 2005, FDA News Digest
• FDA News Digest for April 25, 2005, FDA News Digest
• FDA News Digest for April 18, 2005, FDA News Digest
• FDA News Digest for April 11, 2005, FDA News Digest
• FDA News Digest for April 4, 2005, FDA News Digest
• FDA News Digest for March 28, 2005, FDA News Digest
• FDA News Digest for March 21, 2005, FDA News Digest
• FDA News Digest for March 14, 2005, FDA News Digest
• FDA News Digest for March 7, 2005, FDA News Digest
• FDA News Digest for February 28, 2005, FDA News Digest
• FDA News Digest for February 22, 2005, FDA News Digest
• FDA News Digest for February 14, 2005, FDA News Digest
• FDA News Digest for February 7, 2005, FDA News Digest
• FDA News Digest for January 31, 2005, FDA News Digest
• FDA News Digest for January 24, 2005, FDA News Digest
• FDA News Digest for January 10, 2005, FDA News Digest
• FDA News Digest for January 3, 2005, FDA News Digest
• FDA News Digest for December 20, 2004, FDA News Digest
• FDA News Digest for December 13, 2004, FDA News Digest
• FDA News Digest for December 6, 2004, FDA News Digest
• FDA News Digest for November 29, 2004, FDA News Digest
• FDA News Digest for November 22, 2004, FDA News Digest
• FDA News Digest for November 15, 2004, FDA News Digest
• FDA News Digest for November 8, 2004, FDA News Digest
• FDA News Digest for November 1, 2004, FDA News Digest
• FDA News Digest for October 25, 2004, FDA News Digest
• FDA News Digest for October 18, 2004, FDA News Digest
• FDA News Digest for October 12, 2004, FDA News Digest
• FDA News Digest for October 4, 2004, FDA News Digest
• FDA News Digest for September 27, 2004, FDA News Digest
• FDA News Digest for September 20, 2004, FDA News Digest
• FDA News Digest for September 13, 2004, FDA News Digest
• FDA News Digest for September 7, 2004, FDA News Digest
• FDA News Digest for August 30, 2004, FDA News Digest
• FDA News Digest for August 23, 2004, FDA News Digest
• FDA News Digest for August 16, 2004, FDA News Digest
• FDA News Digest for August 9, 2004, FDA News Digest
• FDA News Digest for August 2, 2004, FDA News Digest
• FDA News Digest for July 26, 2004, FDA News Digest
• FDA News Digest for July 19, 2004, FDA News Digest
• FDA News Digest for July 12, 2004, FDA News Digest
• FDA News Digest for July 6, 2004, FDA News Digest
• FDA News Digest for June 28, 2004, FDA News Digest
• FDA News Digest for June 21, 2004, FDA News Digest
• FDA News Digest for June 14, 2004, FDA News Digest
• FDA News Digest for June 7, 2004, FDA News Digest
• FDA News Digest for June 1, 2004, FDA News Digest
• FDA News Digest for May 3, 2004, FDA News Digest
• FDA News Digest for April 26, 2004, FDA News Digest
• FDA News Digest for April 19, 2004, FDA News Digest
• FDA News Digest for April 12, 2004, FDA News Digest
• FDA News Digest for April 5, 2004, FDA News Digest
• FDA News Digest for March 29, 2004, FDA News Digest
• FDA News Digest for March 22, 2004, FDA News Digest
• FDA News Digest for March 15, 2004, FDA News Digest
• FDA News Digest for March 8, 2004, FDA News Digest
• FDA News Digest for March 1, 2004, FDA News Digest
• FDA News Digest for February 23, 2004, FDA News Digest
• FDA News Digest for February 17, 2004, FDA News Digest
• FDA News Digest for February 9, 2004, FDA News Digest
• FDA News Digest for February 2, 2004, FDA News Digest
• FDA News Digest for January 26, 2004, FDA News Digest
• FDA News Digest for January 20, 2004, FDA News Digest
• FDA News Digest for January 12, 2004, FDA News Digest
• FDA News Digest for January 5, 2004, FDA News Digest
• FDA News Digest for December 22, 2003, FDA News Digest
• FDA News Digest for December 15, 2003, FDA News Digest
• FDA News Digest for December 8, 2003, FDA News Digest
• FDA News Digest for December 1, 2003, FDA News Digest
• FDA News Digest for November 24, 2003, FDA News Digest
• FDA News Digest for November 17, 2003, FDA News Digest
• FDA News Digest for November 10, 2003, FDA News Digest
• FDA News Digest for November 3, 2003, FDA News Digest